Clinical Trials Directory

Trials / Completed

CompletedNCT03493295

Non-interventional, Real Life Study on Satisfaction With LNG-IUS in Spanish Young Women (18-30 Years Old) With Different Parity Status and Menstrual Bleeding Pattern

Status
Completed
Phase
Study type
Observational
Enrollment
587 (actual)
Sponsor
Bayer · Industry
Sex
Female
Age
18 Years – 30 Years
Healthy volunteers
Accepted

Summary

The aim of this non-interventional study (NIS) is to assess, under real-life conditions, woman's satisfaction with Levonogestrel IntraUterine System (LNG-IUS) in a young (18-30 years old (y.o.)) Spanish population taking into account their parity status. Furthermore, the study is aimed to evaluate the impact of: menstrual bleeding pattern and satisfaction with it at baseline, LNG-IUS chosen, previously used contraceptive method and reasons for change to/ choice of a LNG-IUS on overall satisfaction with LNG-IUS use.

Conditions

Interventions

TypeNameDescription
DRUGLevonogestrel IntraUterine System (LNG-IUS)At the routine clinical practice. Jaydess, Mirena, Kyleena Or any other levonogestrel intrauterine system (LNG-IUS) commercialized in Spain at the start of the study, only for contraception indication.

Timeline

Start date
2018-04-25
Primary completion
2020-11-30
Completion
2021-03-15
First posted
2018-04-10
Last updated
2023-11-02

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT03493295. Inclusion in this directory is not an endorsement.